| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:18466740-18466866 | Rare:27 | ||||
| chr20:18466999-18467459 | Common:2; Rare:104 | ||||
| chr20:18507460-18507625 | Rare:43; Clinvar:1 | ||||
| chr20:18507781-18507979 | Common:2; Rare:62; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:18567206-18567499 | Common:4; Rare:95 | ||||
| chr20:19212377-19212546 | Common:2; Rare:55 | ||||
| chr20:19889291-19889574 | Common:2; Rare:57 | ||||
| chr20:20017239-20017410 | Rare:64 | ||||
| chr20:20085306-20085450 | Rare:29 | ||||
| chr20:20712419-20712618 | Common:2; Rare:65 | ||||
| chr20:21125892-21126118 | Common:3; Rare:77 | ||||
| chr20:21303261-21303470 | Rare:71 | ||||
| chr20:21303566-21303851 | Common:1; Rare:81 | ||||
| chr20:23049650-23049939 | Common:3; Rare:94; Clinvar (pathogenic):1 | ||||
| chr20:23086197-23086461 | Common:1; Rare:57 |